Qualitest Pharmaceuticals Issues Voluntary, Nationwide Retail Level Recalls - MPR
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Qualitest Pharmaceuticals Issues Voluntary, Nationwide Retail Level Recalls - MPR
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Tags: Migraine Medication, Pharma, Analgesic Medication, Acetaminophen, Tylenol, Feverall, Tempra, News
Most Recently Shared on June 27, 2011 at 2:25 pm By:
MPR News: Qualitest Pharmaceuticals Issues Voluntary, Nationwide Retail Level Recalls: Qualitest Pharmaceuticals... http://bit.ly/iifu21
Qualitest Pharmaceuticals Issues a Nationwide Voluntary Recall of Oral Contraceptives | Pharmaceutical & Medical Packaging News
pmpnews.com — “, /PRNewswire/ -- Qualitest Pharmaceuticals today issued a voluntary, nationwide, retail-level recall of multiple lots of oral contraceptives.” View full resource at pmpnews.com
Most Recently Shared on September 16, 2011 at 9:09 pm By:
Daphne Allen Health Communicator
Packaging error behind recall of oral contraceptives http://t.co/XbZTpLfr
Qualitest Pharmaceuticals Issues a Nationwide Voluntary Recall of Oral Contraceptives
fda.gov — “Qualitest Pharmaceuticals today issued a voluntary, nationwide, retail-level recall of multiple lots of oral contraceptives. The recall is being implemented because of a packaging error, where select blisters were rotated 180 degrees within the card, reversing the weekly tablet orientation and making the lot number and expiry date no longer visible.” View full resource at fda.gov
Most Recently Shared on September 16, 2011 at 5:42 pm By:
Trish D'Antonio Health Professional
Qualitest Pharmaceuticals Issues a Nationwide Voluntary Recall of Oral Contraceptives: http://t.co/m3cYxOlJ
Qualitest Pharmaceuticals Issues Voluntary, Nationwide Retail Level Recall of Four Lots of Butalbital, Acetaminophen, and Caffeine Tablets, USP 50mg/325mg/40mg and Four Lots of Hydrocodone Bitartrate and Acetaminophen Tablets, USP 7.5mg/500mg
fda.gov — “Qualitest Pharmaceuticals today issued a voluntary nationwide retail level recall of Butalbital, Acetaminophen, and Caffeine Tablets USP, 50mg/325mg/40mg, and Hydrocodone Bitartrate and Acetaminophen Tablets, USP 7.5mg/500mg. This recall was initiated because an individual bottle of Butalbital, Acetaminophen, and Caffeine Tablets USP, 50mg/325mg/40mg, 500 count was found incorrectly labeled with a Hydrocodone Bitartrate and Acetaminophen Tablets, USP 7.5mg/500mg, 1000 count label, printed with L” View full resource at fda.gov
Most Recently Shared on June 26, 2011 at 11:04 pm By:
Qualitest recalls butalbital, acetaminophen and caffeine tablets due to mislabeling http://fb.me/18crWv7X9
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